Canonical Allele Identifier: CA821650063
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1393387054

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612659A>C , CM000668.2:g.1612659A>C GRCh38
NC_000006.11:g.1612894A>C , CM000668.1:g.1612894A>C GRCh37
NC_000006.10:g.1557893A>C NCBI36
NG_009368.1:g.7214A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*552A>C MANE Select ENSP00000493906.1:n.*552A>C
ENST00000380874.3:c.*552A>C ENSP00000370256.2:n.*552A>C
NM_001453.2:c.2214A>C NP_001444.2:n.2214A>C
NM_001453.3:c.*552A>C MANE Select NP_001444.2:n.*552A>C